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8 дней назад

Associate Director, Clinical Science & External Research (MedTech)

137 000 - 235 750$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Director, Clinical Science & External Research (MedTech): Leading end-to-end external research programs, clinical trials, post-market studies, and publication planning for electrophysiology products with an accent on clinical evidence generation, scientific communications, and cross-functional execution. Focus on managing investigator-led research, developing publication strategies, ensuring GCP and ICMJE compliance, and mentoring clinical science staff.

Location: Irvine, California, United States; hybrid work arrangement; up to 15% travel may be required.

Salary: $137,000–$235,750 per year

Company

Johnson & Johnson MedTech develops innovative, less invasive and personalized healthcare solutions, including cardiovascular and electrophysiology products.

What you will do

  • Lead end-to-end management of external research projects, clinical trials and post-market studies.
  • Develop and execute clinical evidence generation and publication strategies with Clinical Research, Biostatistics, investigators and physician authors.
  • Draft and edit scientific publications and presentations while enforcing company policies, SOPs, GCP and ICMJE standards.
  • Coordinate clinical trial procedures, sponsor activities, investigator relationships, study timelines, budgets and management reporting.
  • Partner with Medical Affairs, Data Science, Health Economics and Market Access, Marketing, Education and Communications teams.
  • Supervise and mentor team members and junior Clinical Science & External Research staff.

Requirements

  • Bachelor’s or Master’s degree in Life Science, Physical Science, Nursing, Biological Science or a related field with 10–12 years of relevant experience; or PhD, MD or PharmD with 8–10 years of industry or academic research experience.
  • At least 5 years of clinical research, clinical publication planning and medical writing experience.
  • Experience leading teams in clinical research or evidence generation strategy.
  • Advanced project management, analytical, prioritization and communication skills.
  • Working knowledge of biostatistical methods, Good Clinical Practice and ICMJE standards.
  • Must work from Irvine, California, United States.

Nice to have

  • Medical device experience, particularly cardiovascular or electrophysiology experience.
  • Pre-market or post-market study design and execution experience.
  • Experience with medical writing and publication planning.

Culture & Benefits

  • Inclusive work environment focused on diversity, dignity and equal opportunity.
  • Vacation, sick time, holiday pay, personal and family time, parental leave and caregiver leave.
  • Volunteer leave, bereavement leave and military spouse time off are available according to company policies.
  • Opportunity to collaborate with international teams and external physician partners.

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